SafeStep Huber Needle Set; Catalog Numbers LH-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI 00801741066221), LH-0033 (UDI 00801741066245), LH-0034 (UDI 00801741066269), LH-0035 (UDI 00801741066283), LH-0036 (UDI 00801741066306), LH-0037 (UDI 00801741066320), LH-0038 (UDI 00801741066344), LH-0039 (UDI 00801741066368), LH-0040 (UDI 00801741066382)

Class I - Dangerous

🏥 Medical Devices Recalled: June 19, 2020 Becton Dickinson & Company Surgical Instruments

What Should You Do?

Check if you have this product:
Catalog Numbers LH-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI 00801741066221), LH-0033 (UDI 00801741066245), LH-0034 (UDI 00801741066269), LH-0035 (UDI 00801741066283), LH-0036 (UDI 00801741066306), LH-0037 (UDI 00801741066320), LH-0038 (UDI 00801741066344), LH-0039 (UDI 00801741066368), LH-0040 (UDI 00801741066382). Lot Numbers: ASCYF001 ASCYF017 ASDRF018 ASDRF031 ASDRF040 ASDSF065 ASDSF070 ASDTF004 ASDTF007 ASDVF048 ASDVF054 ASDXF058 ASDXF060 ASDXF066 ASDYF071 ASDYF077 ASDYF098 ASDZF010 ASDZF017 ASDZF024 ASDZF035 ASDZF036 ASDZF046 ASDZF071 ASDZF081 ASDZF093 ASENF002 ASERF025 ASERF032 ASCYF015 ASCYF016 ASCZF027 ASDRF043 ASDRF044 ASDRF054 ASDRF055 ASDRF056 ASDVF058 ASDVF063 ASDXF020 ASDXF045 ASENF011 ASENF014 ASERF004 ASCYF089 ASCYF090 ASCYF091 ASCYF092 ASCZF009 ASCZF010 ASCZF011 ASCZF022 ASCZF023 ASCZF039 ASCZF040 ASCZF045 ASCZF054 ASDPF016 ASDQF035 ASDQF054 ASDQF055 ASDQF060 ASDQF064 ASDRF006 ASDRF014 ASDRF019 ASDRF032 ASDRF039 ASDRF069 ASDRF073 ASDRF087 ASDRF098 ASDSF003 ASDSF010 ASDSF016 ASDSF019 ASDSF022 ASDSF033 ASDSF047 ASDSF050 ASDSF057 ASDSF061 ASDSF069 ASDTF005 ASDTF008 ASDTF022 ASDVF051 ASDVF060 ASDVF071 ASDVF079 ASDVF091 ASDWF004 ASDWF013 ASDWF018 ASDWF034 ASDWF035 ASDWF036 ASDWF040 ASDWF041 ASDWF042 ASDWF046 ASDWF047 ASDWF048 ASDWF052 ASDWF053 ASDWF054 ASDWF058 ASDWF059 ASDWF060 ASDWF080 ASDWF090 ASDWF099 ASDWF121 ASDWF126 ASDXF006 ASDXF014 ASDXF053 ASDXF063 ASDXF070 ASDXF078 ASDXF092 ASDXF096 ASDXF101 ASDXF103 ASDXF106 ASDYF001 ASDYF004 ASDYF006 ASDYF009 ASDYF010 ASDYF015 ASDYF019 ASDYF023 ASDYF029 ASDYF033 ASDYF037 ASDYF044 ASDYF050 ASDYF054 ASDYF060 ASDYF061 ASDYF074 ASDYF082 ASDYF093 ASDZF004 ASDZF013 ASDZF058 ASDZF069 ASEPF012 ASEPF015 ASEPF017 ASEPF021 ASEQF001 ASEQF022 ASEQF026 ASEQF031 ASEQF066 ASEQF083 ASEQF092 ASEQF110 ASEQF132 ASERF013 ASERF022 ASDNF034 ASDNF049 ASDNF055 ASDPF015 ASDPF017 ASDPF021 ASDPF024 ASDPF025 ASDPF026 ASDQF017 ASDRF066 ASDUF120 ASDVF004 ASDVF009 ASDVF013 ASDVF016 ASDVF025 ASDVF028 ASDVF032 ASDVF052 ASDXF048 ASDXF052 ASDXF061 ASDXF068 ASDXF077 ASDXF091 ASDXF100 ASDXF107 ASDYF083 ASDYF088 ASEPF008 ASEPF011 ASEPF014 ASCXF012 ASCXF013 ASDSF006 ASDSF008 ASDSF012 ASDSF013 ASDSF021 ASDSF025 ASDWF110 ASDWF111 ASDWF116 ASDWF122 ASDXF003 ASENF058 ASEQF118 ASCYF011 ASCYF012 ASDRF099 ASDRF100 ASDRF101 ASDSF001 ASDSF005 ASDXF010 ASDXF011 ASDXF016 ASDXF079 ASENF051 ASCYF013 ASCYF014 ASCZF029 ASDVF034 ASDVF035 ASDVF038 ASDVF042 ASDVF044 ASDXF054 ASDXF055 ASENF030 ASENF033 ASENF034 ASENF042 ASCYF010 ASDRF059 ASDRF061 ASDRF062 ASDXF057 ASERF001 ASERF002 ASERF003 ASDQF008 ASDQF009 ASDQF011 ASDQF012 ASDTF100 ASDVF075 ASDXF090 ASDXF093 ASDPF043 ASDPF044 ASDPF045 ASDPF046 ASDQF001 ASDVF077 ASDVF078 ASDXF044 ASDXF047 ASCXF003 ASDSF063 ASDXF080 ASCXF004 ASDPF028 ASDSF064 ASDXF081 ASENF057 Additional lot as of 9/11/20: ASEQF035
Do not eat it: Even if it looks and smells fine, do not consume this product.
Throw it away or return it: You can return the product to the store for a full refund.
Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:: Becton Dickinson & Company
Reason for Recall:: Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
Classification:: Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
Status:: terminated

Product Information

Full Description:

SafeStep Huber Needle Set; Catalog Numbers LH-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI 00801741066221), LH-0033 (UDI 00801741066245), LH-0034 (UDI 00801741066269), LH-0035 (UDI 00801741066283), LH-0036 (UDI 00801741066306), LH-0037 (UDI 00801741066320), LH-0038 (UDI 00801741066344), LH-0039 (UDI 00801741066368), LH-0040 (UDI 00801741066382)

Product Codes/Lot Numbers:

Catalog Numbers LH-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI 00801741066221), LH-0033 (UDI 00801741066245), LH-0034 (UDI 00801741066269), LH-0035 (UDI 00801741066283), LH-0036 (UDI 00801741066306), LH-0037 (UDI 00801741066320), LH-0038 (UDI 00801741066344), LH-0039 (UDI 00801741066368), LH-0040 (UDI 00801741066382). Lot Numbers: ASCYF001 ASCYF017 ASDRF018 ASDRF031 ASDRF040 ASDSF065 ASDSF070 ASDTF004 ASDTF007 ASDVF048 ASDVF054 ASDXF058 ASDXF060 ASDXF066 ASDYF071 ASDYF077 ASDYF098 ASDZF010 ASDZF017 ASDZF024 ASDZF035 ASDZF036 ASDZF046 ASDZF071 ASDZF081 ASDZF093 ASENF002 ASERF025 ASERF032 ASCYF015 ASCYF016 ASCZF027 ASDRF043 ASDRF044 ASDRF054 ASDRF055 ASDRF056 ASDVF058 ASDVF063 ASDXF020 ASDXF045 ASENF011 ASENF014 ASERF004 ASCYF089 ASCYF090 ASCYF091 ASCYF092 ASCZF009 ASCZF010 ASCZF011 ASCZF022 ASCZF023 ASCZF039 ASCZF040 ASCZF045 ASCZF054 ASDPF016 ASDQF035 ASDQF054 ASDQF055 ASDQF060 ASDQF064 ASDRF006 ASDRF014 ASDRF019 ASDRF032 ASDRF039 ASDRF069 ASDRF073 ASDRF087 ASDRF098 ASDSF003 ASDSF010 ASDSF016 ASDSF019 ASDSF022 ASDSF033 ASDSF047 ASDSF050 ASDSF057 ASDSF061 ASDSF069 ASDTF005 ASDTF008 ASDTF022 ASDVF051 ASDVF060 ASDVF071 ASDVF079 ASDVF091 ASDWF004 ASDWF013 ASDWF018 ASDWF034 ASDWF035 ASDWF036 ASDWF040 ASDWF041 ASDWF042 ASDWF046 ASDWF047 ASDWF048 ASDWF052 ASDWF053 ASDWF054 ASDWF058 ASDWF059 ASDWF060 ASDWF080 ASDWF090 ASDWF099 ASDWF121 ASDWF126 ASDXF006 ASDXF014 ASDXF053 ASDXF063 ASDXF070 ASDXF078 ASDXF092 ASDXF096 ASDXF101 ASDXF103 ASDXF106 ASDYF001 ASDYF004 ASDYF006 ASDYF009 ASDYF010 ASDYF015 ASDYF019 ASDYF023 ASDYF029 ASDYF033 ASDYF037 ASDYF044 ASDYF050 ASDYF054 ASDYF060 ASDYF061 ASDYF074 ASDYF082 ASDYF093 ASDZF004 ASDZF013 ASDZF058 ASDZF069 ASEPF012 ASEPF015 ASEPF017 ASEPF021 ASEQF001 ASEQF022 ASEQF026 ASEQF031 ASEQF066 ASEQF083 ASEQF092 ASEQF110 ASEQF132 ASERF013 ASERF022 ASDNF034 ASDNF049 ASDNF055 ASDPF015 ASDPF017 ASDPF021 ASDPF024 ASDPF025 ASDPF026 ASDQF017 ASDRF066 ASDUF120 ASDVF004 ASDVF009 ASDVF013 ASDVF016 ASDVF025 ASDVF028 ASDVF032 ASDVF052 ASDXF048 ASDXF052 ASDXF061 ASDXF068 ASDXF077 ASDXF091 ASDXF100 ASDXF107 ASDYF083 ASDYF088 ASEPF008 ASEPF011 ASEPF014 ASCXF012 ASCXF013 ASDSF006 ASDSF008 ASDSF012 ASDSF013 ASDSF021 ASDSF025 ASDWF110 ASDWF111 ASDWF116 ASDWF122 ASDXF003 ASENF058 ASEQF118 ASCYF011 ASCYF012 ASDRF099 ASDRF100 ASDRF101 ASDSF001 ASDSF005 ASDXF010 ASDXF011 ASDXF016 ASDXF079 ASENF051 ASCYF013 ASCYF014 ASCZF029 ASDVF034 ASDVF035 ASDVF038 ASDVF042 ASDVF044 ASDXF054 ASDXF055 ASENF030 ASENF033 ASENF034 ASENF042 ASCYF010 ASDRF059 ASDRF061 ASDRF062 ASDXF057 ASERF001 ASERF002 ASERF003 ASDQF008 ASDQF009 ASDQF011 ASDQF012 ASDTF100 ASDVF075 ASDXF090 ASDXF093 ASDPF043 ASDPF044 ASDPF045 ASDPF046 ASDQF001 ASDVF077 ASDVF078 ASDXF044 ASDXF047 ASCXF003 ASDSF063 ASDXF080 ASCXF004 ASDPF028 ASDSF064 ASDXF081 ASENF057 Additional lot as of 9/11/20: ASEQF035

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2671-2020

Related Recalls

BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;

Becton Dickinson & Company

Class I - Dangerous

BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.

Oct 14, 2025 Other Medical Devices Nationwide View Details →

PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547

Becton Dickinson & Company

Class I - Dangerous

An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal Saline Flush Syringes with General Pump Compatibility. The use of BD PosiFlush Prefilled Flush Syringes with this stopper causes an increase in injection force, which has the potential to trigger alarms if used with a syringe pump.

Nov 16, 2023 Surgical Instruments Nationwide View Details →

BD gravity sets (Product Name, Catalog #) 32-IN GRAV SET W/0.2 MICRON FILTER BAG ACCESS PORT SS VALVE TEXIUMTM LOW ABSORPTION, Catalog # 4030B-07T and BD GRAVITY BLOOD SET 15 DROP 180 MICRON FILTER SmartSiteTM VALVE NONVENTED, Catalog # 42081E.

Becton Dickinson & Company

Class I - Dangerous

Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).

Oct 11, 2023 Other Medical Devices Nationwide View Details →